BOC-ALA(2-FURYL)-OH DCHA

BOC-ALA(2-FURYL)-OH DCHA - Names and Identifiers

Name	(S)-N-BOC-2-Furylalanine
Synonyms	BOC-ALA(2-FURYL)-OH DCHA (S)-N-BOC-2-Furylalanine BOC-L-2-FURYLALANINE-DCHA Boc-L-2-Furylalanine-DCHA Boc-L-2-Furylalanine·DCHA Boc-3-(2-Furyl)-L-alanine BOC-3-ALA(2-FURYL)-OH DCHA BOC-L-2-FURYLALANINE DCHA SALT boc-l-3-(2-furyl)-alanine·dcha Boc-L-2-Furylalanine Dcha Salt N-tert-Butoxycarbonyl-2-furyl-L-alanine N-(tert-butoxycarbonyl)-3-furan-2-yl-L-alanine BOC-3-(2-FURYL)-L-ALANINE DICYCLOHEXYLAMINE SALT BOC-BETA-(2-FURYL)-L-ALANINE DICYCLOHEXYLAMMONIUM SALT (2S)-2-[(tert-butoxycarbonyl)amino]-3-furan-2-ylpropanoate (2S)-2-[(tert-Butoxycarbonyl)amino]-3-(furan-2-yl)propionic acid 3-(2-furanyl)-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]propanoic acid
CAS	145206-40-2
InChI	InChI=1/C12H17NO5.C12H23N/c1-12(2,3)18-11(16)13-9(10(14)15)7-8-5-4-6-17-8;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h4-6,9H,7H2,1-3H3,(H,13,16)(H,14,15);11-13H,1-10H2/t9-;/m1./s1

BOC-ALA(2-FURYL)-OH DCHA - Physico-chemical Properties

Molecular Formula	C12H17NO5
Molar Mass	255.27
Density	1.2188 (rough estimate)
Boling Point	398.5°C (rough estimate)
Flash Point	307.3°C
Vapor Presure	1.65E-14mmHg at 25°C
Storage Condition	2-8°C
Refractive Index	1.5300 (estimate)

BOC-ALA(2-FURYL)-OH DCHA - Risk and Safety

Hazard Symbols	Xi - Irritant
Safety Description	S24/25 - Avoid contact with skin and eyes.

BOC-ALA(2-FURYL)-OH DCHA - Introduction

(S)-N-BOC-2-Furylalanine(N-tert-butoxycarbonyl-L-3-(2-furyl)alanine) is an organic compound with the following properties:

1. Appearance: (S)-N-BOC-2-Furylalanine is white crystalline powder or crystalline block solid.

2. Solubility: It has poor solubility in common organic solvents and water.

(S)-The main use of N-BOC-2-Furylalanine is as an intermediate and raw material in organic synthesis. It is one of the important starting materials for the synthesis of biologically active compounds or drugs. It can also be used in the preparation of catalysts and metal organic chemical reactions.

The preparation method of this compound is usually carried out through synthetic chemical reactions. Specifically, it can be obtained by esterification of L-3-(2-furyl) alanine in the presence of an N-tert-butoxycarbonylating agent such as tert-butyloxycarbonyl carbamate.

When using or handling (S)-N-BOC-2-Furylalanine should pay attention to the following safety information:

1. (S)-N-BOC-2-Furylalanine may be irritating to the eyes and skin, so wear appropriate protective equipment, such as gloves and goggles, when used.

2. Avoid inhaling the dust or vapor of the compound during operation. Keep well ventilated during storage and use.

3. Use appropriate laboratory procedures and safety measures in a risk-free laboratory environment.

4. If contact or inhalation occurs, immediately rinse skin or eyes with plenty of water and seek medical help.

Last Update：2024-04-09 20:49:11